Quality Control Laboratory Manager

Reposted 17 Days Ago
Be an Early Applicant
Gulfport, MS, USA
In-Office
80K-80K Annually
Senior level
Healthtech • Professional Services • Biotech • Pharmaceutical
The Role
Manage laboratory personnel and ensure compliance with quality control standards, cGMP, and FDA regulations. Oversee functions like audits, training, and equipment management.
Summary Generated by Built In
Allen Spolden is actively recruiting for a Quality Control Laboratory Manager. This is a perm (Direct Hire) opportunity.  Relocation assistance will be provided.

Location: Gulfport, MS (100% onsite is required.)
Work Schedule: M-F, flexible start (4am up to 11am).
Salary: Dependent on experience. 

Job Summary:

The Quality Control Manager is responsible for managing laboratory personnel and maintaining the laboratory to ensure all products and procedures meet the requirements of 21CFR210, 21CFR211, Regulatory Agencies, and customer expectations.

Supervisory Responsibilities:

  • Maintain the laboratory quality management system to ensure compliance with cGMP.
  • Audit the Quality Control Laboratory to ensure compliance to SOP’s.
  • Investigate, assess, and troubleshoot test and/or equipment problems.
  • Review Out-of-trend/Out-of-specification results and participate in investigations to determine root cause and CAPA.
  • Ensure analytical equipment is calibrated and well maintained at all times.
  • Ensure that laboratory personnel training requirements are met and that training records are current.
  • Interview, hire, and train new staff.
  • Provide constructive feedback and retraining as needed.
  • Handles discipline of employees in accordance with company policy.

Duties/Responsibilities:

  • Maintain the laboratory quality management system to ensure compliance with cGMP.
  • Establish product test methods and specifications. This includes raw materials, in-process product, finished products and stability samples.
  • Audit the Quality Control Laboratory to ensure compliance to SOP’s.
  • Maintain appropriate laboratory inventory to ensure timely release of materials.
  • Participate in method qualifications, validations, and transfers.
  • Other duties as assigned.

Required Skills/Abilities:

  • Excellent verbal and written communication skills in English.
  • Excellent management and teamwork skills.
  • Excellent organizational skills and attention to detail.
  • Excellent time management skills with a proven ability to meet deadlines.
  • Ability to function well in a high-paced and at times stressful environment.
  • Ability to understand and follow all Standard Operating Procedures and current Good Manufacturing Practices provided by the Company.
  • Knowledge and control of analytical equipment including calibration and maintenance.
  • Understanding of quality systems including change control, deviations and CAPAs.
  • Ability to handle multiple tasks concurrently and complete them in a timely manner.

Experience:

  • Pharmaceutical Labatory Manager: 5 years (Required)
  • Chemistry/Pharmaceutical: 5 years (Required)
  • CGMP: 5 years (Required)
  • FDA regulations: 5 years (Required)


Requirements

Education and Experience

  • B.S. in Chemistry, Biology, or a related discipline.
  • Experience in computer software, such as Microsoft applications.
  • Good knowledge and understanding of quality control, SOPs, cGMPs, OSHA, and FDA policies and regulations.
  • 10+ years of management experience in a pharmaceutical laboratory setting.
  • Pharmaceutical experience required.

Physical Requirements:

  • Ability to walk, stand, or sit 8 or more hours a day.
  • Ability to lift heavy items up to 40 lbs. or more.

Job Type: Full-time

Pay: $80,000 or more depending on experience



Benefits

Benefits:

  • Dental insurance
  • Health insurance
  • Life insurance
  • Paid time off
  • Vision insurance


Skills Required

  • B.S. in Chemistry, Biology, or a related discipline
  • Pharmaceutical Laboratory Manager: 5 years
  • Chemistry/Pharmaceutical: 5 years
  • CGMP: 5 years
  • FDA regulations: 5 years
  • 10+ years of management experience in a pharmaceutical laboratory setting
  • Good knowledge and understanding of quality control, SOPs, cGMPs, OSHA, and FDA policies and regulations
  • Experience in computer software, such as Microsoft applications
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The Company
0 Employees

What We Do

Allen Spolden specializes in clinical research operations management and provides tailored workforce solutions for clinical research organizations, pharmaceutical, biotech, and healthcare sectors. They offer services in clinical research, data management, regulatory affairs, and talent acquisition.

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